Rimcure 150 mg/400 mg/75 mg filmovertrukne tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

rimcure 150 mg/400 mg/75 mg filmovertrukne tabletter

sandoz a/s - isoniazid, pyrazinamidum, rifampicin - filmovertrukne tabletter - 150 mg/400 mg/75 mg

Rimstar 150+75+400+275 mg filmovertrukne tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

rimstar 150+75+400+275 mg filmovertrukne tabletter

sandoz a/s - ethambutolhydrochlorid, isoniazid, pyrazinamidum, rifampicin - filmovertrukne tabletter - 150+75+400+275 mg

Namuscla Den Europæiske Union - dansk - EMA (European Medicines Agency)

namuscla

lupin europe gmbh - mexiletine hydrochloride - myotonic lidelser - hjertetapi - namuscla er indiceret til symptomatisk behandling af myotonia i voksne patienter med ikke-dystrofiske myotonic lidelser.

Talzenna Den Europæiske Union - dansk - EMA (European Medicines Agency)

talzenna

pfizer europe ma eeig - talazoparib - bryst neoplasmer - antineoplastiske midler - talzenna er angivet som monoterapi til behandling af voksne patienter med germline brca1/2 mutationer, der har her2-negative lokalt fremskreden eller metastatisk brystkræft. patients should have been previously treated with an anthracycline and/or a taxane in the (neo)adjuvant, locally advanced or metastatic setting unless patients were not suitable for these treatments. patienter med hormon receptor (hr)-positiv brystkræft skulle have været behandlet med en forudgående endokrine-baseret terapi, eller anses uegnet til at endokrine-baseret terapi.

Rimstar 150+75+400+275 mg filmovertrukne tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

rimstar 150+75+400+275 mg filmovertrukne tabletter

orifarm a/s - ethambutolhydrochlorid, isoniazid, pyrazinamidum, rifampicin - filmovertrukne tabletter - 150+75+400+275 mg

Xospata Den Europæiske Union - dansk - EMA (European Medicines Agency)

xospata

astellas pharma europe b.v. - gilteritinib fumarate - leukæmi, myeloid, akut - antineoplastiske midler - xospata er angivet som monoterapi til behandling af voksne patienter med recidiverende eller refraktær akut myeloid leukæmi (aml) med en mutation flt3.

Jyseleca Den Europæiske Union - dansk - EMA (European Medicines Agency)

jyseleca

gilead sciences ireland uc, galapagos nv - filgotinib maleate - arthritis, reumatoid - immunosuppressiva - rheumatoid arthritisjyseleca is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease modifying anti rheumatic drugs (dmards). jyseleca may be used as monotherapy or in combination with methotrexate (mtx). ulcerative colitisjyseleca is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic agent.

Rifampar 150+75+400+275 mg filmovertrukne tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

rifampar 150+75+400+275 mg filmovertrukne tabletter

paranova danmark a/s - ethambutolhydrochlorid, isoniazid, pyrazinamidum, rifampicin - filmovertrukne tabletter - 150+75+400+275 mg